sumatriptan

Generic: sumatriptan

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler rising pharma holdings, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 50 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-661
Product ID 64980-661_44569522-5e18-4e73-bb20-cac2c0f7a12f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219036
Listing Expiration 2026-12-31
Marketing Start 2025-05-05

Pharmacologic Class

Classes
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa] serotonin-1b and serotonin-1d receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64980661
Hyphenated Format 64980-661

Supplemental Identifiers

RxCUI
313160 313161 315223
UPC
0364980661362 0364980660365 0364980662369
UNII
J8BDZ68989

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sumatriptan (source: ndc)
Generic Name sumatriptan (source: ndc)
Application Number ANDA219036 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (64980-661-27) / 9 TABLET, FILM COATED in 1 BLISTER PACK
  • 36 TABLET, FILM COATED in 1 BOTTLE (64980-661-36)
  • 1 BLISTER PACK in 1 CARTON (64980-661-91) / 9 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (3)

64980-661-27 3 BLISTER PACK in 1 CARTON (64980-661-27) / 9 TABLET, FILM COATED in 1 BLISTER PACK 64980-661-36 36 TABLET, FILM COATED in 1 BOTTLE (64980-661-36) 64980-661-91 1 BLISTER PACK in 1 CARTON (64980-661-91) / 9 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

sumatriptan succinate (50 mg/1)

Linked Drug Pages (1)

sumatriptan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44569522-5e18-4e73-bb20-cac2c0f7a12f", "openfda": {"upc": ["0364980661362", "0364980660365", "0364980662369"], "unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["352d2ab3-d2c7-48c8-bcd4-d46ed9bdfa85"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (64980-661-27)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "64980-661-27", "marketing_start_date": "20250505"}, {"sample": false, "description": "36 TABLET, FILM COATED in 1 BOTTLE (64980-661-36)", "package_ndc": "64980-661-36", "marketing_start_date": "20250723"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (64980-661-91)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "64980-661-91", "marketing_start_date": "20250505"}], "brand_name": "sumatriptan", "product_id": "64980-661_44569522-5e18-4e73-bb20-cac2c0f7a12f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "64980-661", "generic_name": "sumatriptan", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA219036", "marketing_category": "ANDA", "marketing_start_date": "20250505", "listing_expiration_date": "20261231"}